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ALAS2 Protéine

ALAS2 Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 85 % as determined by reducing SDS-PAGE.
N° du produit ABIN7319672
  • Antigène Voir toutes ALAS2 Protéines
    ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))
    Type de proteíne
    Recombinant
    Origine
    • 4
    • 1
    • 1
    Humain
    Source
    • 2
    • 2
    • 1
    • 1
    Escherichia coli (E. coli)
    Fonction
    Recombinant Human Catalase/CAT Protein
    Séquence
    Ala2-Leu527
    Attributs du produit
    Recombinant Human Catalase is produced by our E.coli expression system and the target gene encoding Ala2-Leu527 is expressed.
    Pureté
    > 85 % as determined by reducing SDS-PAGE.
    niveau d'endotoxine
    < 1.0 EU per μg as determined by the LAL method.
    Top Product
    Discover our top product ALAS2 Protéine
  • Restrictions
    For Research Use only
  • Format
    Frozen, Liquid
    Buffer
    Supplied as a 0.2 μm filtered solution of 20 mM PB,150 mM NaCl, pH 7.4.
    Stock
    -20 °C
    Stockage commentaire
    Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.
  • Antigène
    ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))
    Autre désignation
    alase (ALAS2 Produits)
    Synonymes
    anh1 Protein, asb Protein, xlsa Protein, ALAS-E Protein, ALASE Protein, ANH1 Protein, ASB Protein, XLDPP Protein, XLEPP Protein, XLSA Protein, alas-e Protein, cb1063 Protein, sau Protein, sauternes Protein, ALAS Protein, Alas-2 Protein, 5'-aminolevulinate synthase 2 Protein, aminolevulinate, delta-, synthase 2 Protein, aminolevulinic acid synthase 2, erythroid Protein, alas2 Protein, ALAS2 Protein, Alas2 Protein, alas2.L Protein
    Sujet

    Background: Catalase (CAT) is a member of the catalase family. It exists as a homotetramer that occurs in almost all aerobically respiring organisms and serves to protect cells from the toxic effects of hydrogen peroxide. Catalase is localized in the peroxisome. Catalase promotes growth of cells including T-cells, B-cells, myeloid leukemia cells, melanoma cells, mastocytoma cells, and normal and transformed fibroblast cells. Defects in CAT are the cause of acatalasemia which is characterized by absence of catalase activity in red cells and is associated with ulcerating oral lesions.

    Synonym: MGC138422,MGC138424

    Poids moléculaire
    59.7 kDa
    UniProt
    P04040
    Pathways
    Transition Metal Ion Homeostasis
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